agarose electrophoresis 中文意思是什麼
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The result of the agarose gel electrophoresis showed that the length of the full - length cdnas in the library was pooled mainly between 500 and 2 000 base pairs
結果表明獲得的ejoi基因的cdna長度為876hp ，開放閱讀框長度為759hp ，編碼252個氨基酸。 -
Apoptotic peak. agarose gel electrophoresis showed that 185 - base pair ladder characteristic of the dna degradation that occurs in apoptotic cells induced by a
電泳出現階梯狀條帶流式細胞儀檢測出現典型的凋亡峰，提示 -
The apoptosis induced by extract of russula subnigricans hongo was investigated in little white rat liver and kidney cells by agarose gel electrophoresis. the result showed that agarose gel electrophoresis of dna extracted from poisoned little white rat liver and kidney cells revealed typical 180 ~ 200bp integer - fold " ladder " " bands. apoptosis induced by extract of russula subnigricans hongo was dose - and time - dependentthe result indicated that extract of russula subnigricans hongo could induce apoptosis in little white rat liver and kidney cells
4 .用電泳技術研究亞稀褶黑菇粗毒液誘導小白鼠肝腎細胞凋亡，小白鼠亞稀褶黑菇抽提液中毒后，肝腎細胞. dna經瓊脂糖凝膠電泳出現180一200bp整數倍的ona梯形帶， 19 . 09 / l一28 . 59 / l范圍內，亞稀褶黑菇提取液誘導肝腎細胞凋亡表現出時間和劑量依賴性 -
The biological characteristics and toxicity of russula subnigricans hongo was studied for the first time from ecology and morphologic characteristics and histology, the orthogonal experiment of the optimum culture condition, the analysis of components, apoptosis of the cells from little white rat liver and kidney induced by extract of russula subnigricans hongo, to the histopathologic changes observation of little white rat liver and kidney through ecological observation, light microscopy and scanning electron microscopy, reversed - phase high performance liquid chromatography, agarose gel electrophoresis, transmission electron micioscopy. the result showed as below : based on ecological observation of russula subnigricans hongo, its ecological environment was investigated in order to simulate its ecological environment when they are cultivated
利用菌種分離技術、光鏡技術、電鏡技術、高效液相色譜技術、毒理實驗技術、電泳方法等對亞稀褶黑菇（ russulasubnigricanshongo ）的生物學特性和毒性機理進行了研究，主要包括以下內容：亞稀褶黑菇的生態學和組織學研究、菌種分離培養、掃描電鏡觀察、成分分析、粗毒液誘導小自鼠肝腎細胞凋亡，小白鼠中毒后肝腎細胞透射電鏡觀察，研究結果如下： 1 -
I and hindlll respectively. after the digested products were run via agarose gel electrophoresis and transferred into nylon membrane, the southern blot was carried out using the cdna of rubber tree etrl as probe. the result of the southern blot showed that a hybridization band ( - 3. 0kb ) turned up from the ecor i digested product and another band ( - 4. 8kb ) turned up from the hindi ]
從橡膠樹pr107品系的嫩葉提取基因組dna ，用限制性內切酶ecor 、 hinofll分別酶切，瓊脂糖凝膠電泳分離並轉膜后，用克隆的橡膠樹etri基因的cdna片段作探針進行southern雜交分析，結果表明， ecor酶切在約3 okb處有一條雜交帶出現， hi 。 -
Dna ladder bands with a periodicity of about 200 bp were clearly seen in agarose gel electrophoresis pattern
瓊脂糖凝膠電泳基因組dna可見到約以200bp為間隔的dna梯狀（ ladder ）條帶。 -
Methods : the effects of different neurotrophic factors on the growth and differentiation of neural stem cells were observed by cells counting and immunofluorescence staining. the levels of rara mrna and rxra mrna in differentiated neural stem cells were assayed by rt - pcr. agarose gel electrophoresis and image analysis
方法應用細胞計數和免疫熒光細胞化學法，研究不同神經營養因子對神經幹細胞增殖及分化的影響；應用rt - pcr 、瓊脂糖凝膠電泳和紫外分光圖象分析法檢測神經幹細胞分化過程中rar和rxr mrna表達量的改變。結果1 -
It has marked apoptotic induction on mouse spleen cells tested by dna agarose gel electrophoresis analysis and flow cytometric assay in certain degree. it also can decrease the activity of lactate dehydrogenase ( ldh ) outside of mouse the spleen cells and increase the quantity of reduced gsh inside the mouse spleen cells
而且一定濃度范圍內可引起小鼠脾淋巴細胞dna發生特徵性降解，出現dnaladders ，引起染毒組細胞凋亡率顯著性升高，但細胞凋亡率與劑量不呈直線相關關系。 -
A final period of extension was carried out for 9 min and final holding at 4. the pcr products were resolved after electrophoresis in 2 % agarose gel with ethidium bromide. the pcr products were visualized while the gel was exposed to ultraviolet light
擴增產物在2瓊脂糖凝膠上電泳，用pcrmarker作分子量標準，紫外燈下觀察，最適pcr反應條件為擴增出最強的sry產物帶而無非特異性擴增帶出現時的反應條件。 -
To construct eukaryotic expression vector of mbl gene with codon 54 point mutation, the target sequence in pgem - mbld plasmid, which conains mbl cdna with codon 54 mutant allele, was amplified by pcr. after the cdna fragement and plasmids pci - neo were prepared by digestion with sma i and sal i, the fragment was inserted into sma i and sal i site in pci - neo eukaryotic expression vector, and the recombinant vector, named pci - mbl54, was obtained. the pci - mbl54, digested with restriction enzymes, was found to contain the point mutation mbl cdna by agarose gel electrophoresis analysis
本實驗以ggc54gacmbl突變為研究對象，選用真核表達質粒pci - neo ，根據已構建好的含54位密碼子突變型mbl基因t載體的結構，設計合成新的引物， pcr擴增54位密碼突變型mbl基因，凝膠回收，雙酶切pcr產物和pci - neo質粒， t4連接酶連接，將前者克隆至後者的sma和sal位點，轉化大腸桿菌xl - 1blue ，氨芐選擇培養。 -
The high purity of genomic dna extracted by tripure isolation reagent was observed. dna agarose gel electrophoresis showed that the genome had a high integrity without degradation. and also, spectrophotometric analysis indicated that the genomic dna had no pollution by protein and rna. 2
培養乳酸乳球菌nizor5 ，收集菌體，用tripurelsolationreagent提取其基因組dna ，瓊脂糖凝膠電泳，紫外顯示儀下可見在點樣孔附近有一條整齊均一的dna帶。 -
A dna band about 1700 bp in length was found in the rt - pcr products of both strains after an agarose - gel electrophoresis, which was consistent with the length of hn registered in genbank
瓊脂糖電泳結果顯示，其大小均約為1700bp ，與genbank登錄的大小一致。其次，將hn基因cdna定向插入pcdna3中。 -
Application and evaluation of hemoglobin agarose electrophoresis in - thalassemia
地中海貧血中的應用及評價 -
Agarose gel electrophoresis video clip wmv format, window media player required
瓊脂糖凝膠電泳示範片段wmv格式，需用window media player播放 -
Agarose gel electrophoresis
瓊脂糖凝膠電泳 -
Methods : cross electrophoresis of agarose - starch mixed gel was used in this experiment
方法：澱粉瓊脂糖混合凝膠交叉電泳。
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